US4469748A - Adhesion of aramid cords to rubber - Google Patents
Adhesion of aramid cords to rubber Download PDFInfo
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- US4469748A US4469748A US06/510,715 US51071583A US4469748A US 4469748 A US4469748 A US 4469748A US 51071583 A US51071583 A US 51071583A US 4469748 A US4469748 A US 4469748A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
- C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M10/00—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements
- D06M10/02—Physical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. ultrasonic, corona discharge, irradiation, electric currents, or magnetic fields; Physical treatment combined with treatment with chemical compounds or elements ultrasonic or sonic; Corona discharge
- D06M10/025—Corona discharge or low temperature plasma
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2321/00—Characterised by the use of unspecified rubbers
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
- D06M2101/36—Aromatic polyamides
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- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M2200/00—Functionality of the treatment composition and/or properties imparted to the textile material
- D06M2200/50—Modified hand or grip properties; Softening compositions
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S156/00—Adhesive bonding and miscellaneous chemical manufacture
- Y10S156/91—Bonding tire cord and elastomer: improved adhesive system
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2938—Coating on discrete and individual rods, strands or filaments
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/29—Coated or structually defined flake, particle, cell, strand, strand portion, rod, filament, macroscopic fiber or mass thereof
- Y10T428/2913—Rod, strand, filament or fiber
- Y10T428/2933—Coated or with bond, impregnation or core
- Y10T428/2964—Artificial fiber or filament
- Y10T428/2967—Synthetic resin or polymer
- Y10T428/2969—Polyamide, polyimide or polyester
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T442/00—Fabric [woven, knitted, or nonwoven textile or cloth, etc.]
- Y10T442/30—Woven fabric [i.e., woven strand or strip material]
- Y10T442/3854—Woven fabric with a preformed polymeric film or sheet
- Y10T442/3911—Natural or synthetic rubber sheet or film
Abstract
An aramid reinforcing element is treated with a cold gas plasma of air, N2, He, Ne or Ar or mixture thereof at up to 300 watts power for a few seconds to several minutes to improve its adhesion to rubber compounds.
Description
This invention relates to the adhesion of aramid reinforcing elements such as cords, fabric or fibers to rubber.
Gas plasma basically consists of highly excited gas/vapor species (i.e., molecules, ions, free radicals) produced by bombarding gases with energy. Some familiar examples of gas plasma are sun (thermal plasma) and neon signs (cold plasma). The temperature of the constituents in the thermal plasma is in the thousands of degrees, whereas in the cold plasma, the temperature is from ambient to a few hundred degrees. Corona discharges lie in between these two plasmas and may be termed hybrid plasmas.
The use of cold plasma for the "surface modification" of polymers has increased significantly during the past 10-15 years. The desired surface modifications have included increased wettability1-4, hydrophilicity5 and bonding1,2,4,6. Other areas have included the grafting of monomers onto polymer surfaces7-10 and the deposition of thin protective coatings of organic and inorganic precursors on metal11-13 and polymer surfaces14. A number of papers on the surface modification of polymers by corona discharge treatment have also appeared15-19.
Cold plasma treatment for surface modification can be divided into the following classes according to the type of vapor and procedure employed6 :
I. Chemically inert plasma using Ar, He, etc.
II. Nonpolymerizable reactive-gas plasmas using N2, NH3, air etc.
III. "Grafting" plasmas in which the substrate is first activated in an Ar plasma and then immediately exposed to a polymerizable vapor in the absence of plasma.
IV. "Polymerizable" reactive gas plasmas which can employ both unsaturated and saturated hydrocarbons, and organometallic molecules. The resulting polymer coatings in such cases are usually significantly different from the precursors both in molecular structure and composition. This is because the "polymerization" process in this case involves considerable fragmentation of the precursors and recombination of some of the fragments. Ablation of the deposited coating can also be important in this case.
Needless to say, the first two of the above are the simplest of the cold plasma surface treatments. While limited in scope, they have been shown to result in significant adhesion improvement of the treated substrates. It was found that treatment of poly(monochloro-p-xylene) in Ar, He and O2 plasma increased its adhesion to urethane coatings by a factor of ten over the untreated control4. Power levels used were 50-100 watts and treatment times ranged from 1-6 minutes. Water contact angles were found to decrease in all cases, but in the case of O2 plasma, oxygen was found to be incorporated into the surface polymer. Interestingly, Ar and He treatments gave somewhat higher adhesions than the oxygen treatment. The beneficial effects of plasma treatment were found to persist in at least up to one week of storage before application of a urethane coating.
Treatment of non-adhesive activated polyester (PET) filaments and cords in various gas plasmas (N2, Ar, He, H2, NH3, H2 O, CO2, O2) was found to increase cord-RFL rubber H-adhesion by about 100% over the untreated control2. Plasma treatment of PET, therefore, could replace a primer treatment in a two-step polyester dip system. All of the above gases gave essentially equivalent adhesion improvement. Power levels used were 75-275 watts and treatment times ranged from 4-34 seconds. Gas pressures were between 0.5-1.5 torr. A number of patents20,21 claiming the use of plasma treatment for adhesion improvement in polyester cord-RFL-rubber system have issued.
It has been proposed that the increase in adhesion of polyester to rubber after plasma treatment resulted from crosslinking of the surface region inducing increased cohesive strength near the interface23,24. It, also, has been proposed that plasma treatment might have three effects: (1) increase in the potential for strong bonding by introducing polar groups, free radicals, etc., at the polymer surface; (2) increase in surface crosslinking and the contaminant energy dissipation; and (3) increase in elastic modulus through crosslinking25.
Plasma treatment of KEVLAR for adhesion to epoxy resin gave up to 120% improvement in the peel strength adhesion of KEVLAR-epoxy laminates as a result of the plasma treatment6,22. All four classes of plasma described above were used. Generally Ar, N2, NH3 and air plasmas gave improvements of 30-80% in these studies. No adhesion studies for KEVLAR-rubber systems were carried out by these authors.
An object of this invention is to provide a process for adhering or binding rubber to aramid fibers or reinforcing elements providing an increased adhesive bond between the aramid fibers and rubber. Another object is to provide aramid cords, fibers, fabric or reinforcing elements with a minor amount by weight of an adhesive so that subsequently said adhesive coated element may be bonded to rubber. A further object is to provide a composite of an aramid reinforcing element bonded to a rubber compound. These and other objects and advantages of the present invention will become more apparent to those skilled in the art from the following detailed description and working examples.
It has been found that cold plasma treatment of aramid fibers such as KEVLAR tire cords before application of the adhesive leads to an improvement in adhesion of the treated, dipped cord to rubber relative to the cords which are not plasma treated before dipping. The relative level of improvement depends on the type of adhesive used and can vary from about 10 to about 50%. An improvement of about 25-30% in KEVLAR-rubber adhesion results if the plasma treated undipped cord is compared to the untreated undipped control cord. Furthermore, the results obtained show that for plasma treated, dipped cords the mode of failure is predominantly through rubber tear. This suggests that the percentage improvement in cord-rubber bond strength as a result of plasma treatment may actually be higher than shown by the measurements used.
The aramid cords are treated in a cold gas plasma at from about 10 to 300, preferably from about 25 to 75, watts of power for from about 2 seconds to 30 minutes, preferably from about 2 to 20 minutes. These ranges can vary somewhat depending on the equipment size and loading of the equipment with the material to be treated but sufficient to enable improvement in adhesion of the cord to rubber. The gas used can be air, nitrogen, helium, neon or argon or mixture thereof; preferably the gas is nitrogen or argon. After plasma treatment the cords are dipped in a cord dip of a vinyl pyridine copolymer latex and a thermosetting water soluble phenolic-aldehyde resin, dried, embedded in a vulcanizable rubber compound and cured.
The aramid used as a reinforcing element in the practice of the present invention is poly(p-phenylene terephthalamide), e.g. ##STR1## where n is a number. It is known as KEVLAR and is manufactured by the duPont Company. The aramid reinforcing element may be in the form of fibers, continuous filaments, staple, tow, yarns, cords (preferred), fabric and so forth.
The water soluble thermosetting (heat reactable) phenolic-aldehyde resin is made by reacting an aldehyde with a phenolic compound. The preferred aldehyde to use is formaldehyde, but acetaldehyde and furfural, also, may be used. In place of formaldehyde one may use paraformaldehyde or other formaldehyde donors such as hexamethylenetetramine and so forth. Also, it is preferred to start with formalin, usually a 37% solution of formaldehyde in water, which is easier to use. Mixtures of aldehydes can be used. The phenolic compound can be phenol itself, resorcinol, the cresols, the xylenols, p-tert butylphenol or p-phenyl phenol or mixture thereof. Mixtures of resins can be used. If a phenol-aldehyde resin is used, some resorcinol and/or resorcinol-aldehyde resin should be added to prevent or reduce tackiness. The reactants are reacted in water usually in the presence of a catalyst. One may start with a thermoplastic resin by reacting less than a molar amount of the aldehyde with the phenolic to form a condensation product and then may add sufficient aldehyde at the time the dip is formulated to convert the product to a thermosetting or infusible resin on heating. Alternatively, one may react a molar excess of the aldehyde with the phenolic to form a thermosetting type condensation product on heating and which should be used promptly. In any event, the final product on heating is a thermoset phenolic-aldehyde resin. Information on the preparation of the water soluble thermosetting phenolic-aldehyde resins will be found in "Encyclopedia of Chemical Technology," Kirk-Othmer, Volume 15, Second Edition, 1968, Interscience Publishers Division of John Wiley & Sons, Inc., New York, pages 176 to 208; "Technology of Adhesives," Delmonte, Reinhold Publishing Corp., New York, N.Y., 1947, pages 22 to 52; "Formaldehyde," Walker, A.C.S. Monograph Series, Reinhold Publishing Corp., New York, N.Y., Third Edition, 1964, pages 304 to 344 and "The Chemistry of Phenolic Resins," Martin, John Wiley & Sons, Inc., New York, 1956.
Rubbery aqueous alkaline vinyl pyridine copolymer latices are well known. See U.S. Pat. Nos. 2,561,215; 2,615,826; 3,437,122; 4,145,494; 4,251,409 and 4,285,850. They comprise a copolymer of about 50 to 95% by weight of butadiene-1,3, 5 to 40% by weight of a vinyl pyridine, and 0 to 40% by weight of a vinyl aromatic compound like styrene. Examples of suitable vinyl pyridines are 2-vinyl pyridine, 4-vinyl pyridine, 2-methyl-5-vinyl pyridine and 5-ethyl-2-vinyl pyridine. It is usually preferred to use a latex of a terpolymer of from about 60 to 80% by weight of butadiene-1,3, from about 7 to 32% by weight of styrene and from about 4 to 22% by weight of 2-vinyl pyridine. Even more preferred is a terpolymer of about 70% by weight of butadiene-1,3, 15% styrene and 15% 2-vinyl pyridine. Part of the vinyl pyridine copolymer may be replaced with a rubbery butadiene-styrene copolymer and/or a rubbery polybutadiene so long as the relative ratios between the butadiene-1,3, vinyl pyridine and styrene remain as set forth above.
The rubbery vinyl pyridine copolymer and the rubbery polybutadiene or rubbery butadiene copolymer are made in water using free radical catalysts, chelating agents, modifiers, emulsifiers, surfactants, stabilizers, short stopping agents and so forth. They may be hot or cold polymerized, and polymerization may or may not be carried to about 100% conversion. If polymerizations are carried out with appropriate amounts of chain transfer agents or modifiers and conversions are stopped below 100% conversion, low or no gel polymers are possible. Free radical aqueous emulsion polymerization is well known as shown by:
(1) Whitby et al, "Synthetic Rubber," John Wiley & Sons, Inc., New York, 1954;
(2) Schildknecht, "Vinyl and Related Polymers," John Wiley & Sons, Inc., New York, 1952;
(3) "Encyclopedia of Polymer Science and Technology," Interscience Publishers a division of John Wiley & Sons, Inc., New York, Vol. 2 (1965), Vol. 3 (1965), Vol. 5 (1966), Vol. 7 (1967) and Vol. 9 (1968) and
(4) Bovey et al, "Emulsion Polymerization," Interscience Publishers, Inc., New York, 1955.
In addition to the surfactants or wetting agents, and any antioxidants already in the latex, additional surfactants, antioxidants and antidegradants may be added to the resin-latex dip in minor amounts.
The pH of the latex and of the dips should be on the alkaline side and the pH of any surfactants and stabilizers, including freeze-thaw stabilizers and other additives should be on the alkaline side or compatible or be neutral to avoid improper coagulation of the latex or latices.
Water is used in the adhesive phenolic-aldehyde/latex dip in an amount sufficient to provide for the desired dispersion of the rubber or latex particles, and for the solution of the resin and any other additives, to obtain the desired viscosities, and for the proper solids content to get the necessary pickup of solids on and penetration between the fibers of the cord. The amount of water in the adhesive cord dip generally may vary so as to provide a solids content of from about 10 to 50%, preferably from about 20 to 25%, by weight. Too much water may require use of excess heat to evaporate the water on drying. Too little water may cause uneven penetration or too slow coating speeds.
On a dry weight basis the phenolic-aldehyde resin is used in an amount of about 3 to 25, preferably from about 6 to 20, parts by weight per 100 parts by weight of the rubber of the latex of the dip.
To apply the resin/latex dip to the plasma treated aramid fiber cords in a reliable manner, the cords are fed through the adhesive dip bath while being maintained under a small predetermined tension and into a drying oven where they are dried under a small predetermined tension (to prevent sagging without any appreciable stretching). As the cords leave the oven they enter a cooling zone where they are air cooled before the tension is released. In each case the adhesive-coated cords leaving the dip are dried (cured or heat set) in the oven at from about 200° to 600° F. (93.3° to 315.6° C.) for from about 300 to 5 seconds. The time the cord remains in the adhesive is about a few seconds or more or at least for a period of time sufficient to allow wetting of the cord and at least some impregnation of the fibers of the cord. Successive treatments if desired, e.g., dipping and drying with the resin/latex dips, may be conducted in the same fashion.
The single-cord H-pull, H-adhesion, test is employed to determine the static adhesion of the dried (heat set or cured) adhesive coated plasma treated aramid fiber cords to rubber. In each case the rubber test specimens are made from a vulcanizable rubber composition comprising rubber, reinforcing carbon black and the customary compounding and curing ingredients. In every case the cords to be tested are placed in parallel positions in a multiple-strand mold of the type described in the single-cord H-pull adhesion test ASTM designated D 2138-72, the mold is filled with the unvulcanized rubber composition, the cords being maintained under a tension of 50 grams each, and the rubber is cured. Each rubber test specimen is 1/4 inch thick and has a 3/8 inch cord embedment. After the rubber has been cured, the hot cured rubber piece is removed from the mold, cooled and H-test specimens are cut from said piece, each specimen consisting of a single cord encased in rubber and having each end embedded in the center of a rubber tab or embedment having a length of around 1 inch or so. The specimens are then aged at least 16 hours at room temperature. The force required to separate the cord from the rubber is then determined at room temperature (about 25° C.) or at 250° F. (121° C.) using an INSTRON tester provided with specimen grips. The maximum force in pounds required to separate the cord from the rubber is the H-adhesion value. All the data submitted in the working examples which follow are based upon identical test conditions, and all of the test specimens were prepared and tested in the same way generally in accordance with ASTM Designation: D 2138-72.
Plasma treated aramid cords or fabric coated with the adhesive dips of the present invention can have up to about 20%, preferably up to about 15%, total by weight (dry) solids (pick up) of the adhesive dip, including a primer if used, on the cord based on the weight of the cord and can be used in the manufacture of carcasses, belts, flippers and chafers of radial, bias, or belted-bias passenger tires, truck tires, motorcycle tires, off-the-road tires and airplane tires, and, also, in making transmission belts, V-belts, conveyor belts, hose, gaskets, tarpaulins and the like.
While the adhesive containing plasma treated aramid fiber reinforcing element can be adhered to vulcanizable natural rubber, rubbery butadiene-styrene copolymer or rubbery polybutadiene or blend thereof by curing the same in combination together, it is apparent that the heat cured adhesive containing plasma treated aramid fiber reinforcing element can be adhered to other vulcanizable rubbery materials, by curing or vulcanizing the same in combination with the rubber, such as one or more of the foregoing rubbers as well as nitrile rubbers, chloroprene rubbers, polyisoprenes, acrylic rubbers, isoprene-acrylonitrile rubbers and the like and mixtures of the same. These rubbers can be mixed with the usual compounding ingredients including sulfur, stearic acid, zinc oxide, magnesium oxide, silica, carbon black, accelerators, antioxidants, antidegradants and other curatives, rubber compounding ingredients and the like well known to those skilled in the art for the particular rubbers being employed.
The following examples will serve to illustrate the present invention with more particularity to those skilled in the art. In these examples parts are parts by weight unless otherwise noted.
PLASMOD (Tegal Corporation, Novato, Calif.) unit (26.7 cm. high, 30 cm wide, 37.6 cm long and weighing 32 lbs.) was used for plasma treatment. It consisted of a pyrex glass reaction chamber 15 cm long and 10.54 cm inside diameter. Power for plasma generation was supplied by two semi-cylindrical electrodes mounted all around the reaction chamber. The RF (radio frequency) power generator was a crystal controlled oscillator designed to provide up to 100 watts of continuous wave 13.56 MHz (mandated by FCC) power to the reaction chamber. Power output was controlled by a calibrated dial.
The gas/vapor was delivered to the reaction chamber through a delivery tube containing perforations (the part inside the chamber) to allow for even gas distribution. Provision was made to evacuate the chamber (cold plasma is a low pressure process). The vacuum valve was controlled in series with the RF generator switch to prevent RF power from coming on unless the chamber was evacuated. Accessories included a flow meter (Cole-Parmer FM062-01ST), a vacuum indicator (Labconco Model No. 75800) and a vacuum pump (Duo Seal, H. M. Welch Manufacturing Co.).
A rectangular frame (14.5 cm long and 8.5 cm wide) was built from stainless steel tubing (0.63 mm nominal diameter) to string cords for placement in the plasma reaction chamber. Small holes about 0.8 cm apart were drilled and tapped along the two shorter sides and thin screws were inserted. A maximum of about 3.3 meters of cord could be strung on each frame and up to three such frames could be stacked in the chamber. A cord length of one meter was considered to be the minimum required for dipping and H-adhesion testing. Because of the nature of the frame, a number of cord-frame contact points (about 14 cm apart each) were involved and one side of the cord at these points may not have received the same level of plasma treatment as the rest of the cord. While this may have resulted in some adhesion variability, it was felt that this method of cord placement was better than placing the cord in a container as a loose bundle for plasma treatment.
Cord: KEVLAR (1500/3, poly(p-phenylene terephthalamide), ##STR2## where n is a number), greige, as received from duPont.
Gases: N2 and Ar--High purity grade as received from Akron Oxygen Company.
At the start of each day, the plasma unit was turned on to allow the tubes to warm up for at least fifteen minutes. The vacuum pump was then turned on and the chamber evacuated to <0.01 torr. Gas (N2 or Ar) was then turned on and after the pressure had stabilized at about 1 torr, the RF power was turned on (50 watts level) to "burn off" any contaminants left in the chamber. After about 30 minutes of cleaning, the unit was considered ready for experimentation. The unit was tuned at the desired flow rate and power level with a dummy frame in place before beginning plasma treatments.
The frame containing the cords was placed in the reaction chamber and the chamber was evacuated for 2 minutes. Gas flow was turned on and the chamber pressure was recorded. RF power was turned on to generate the plasma and after the required treatment time, the power was turned off. Gas flow was stopped and the chamber was evacuated for 5 minutes. The vacuum valve was then turned off and the sample removed for dipping. Gas flow rates were varied between 40-100 ml/minute and the treatment times were between 0.2-20 minutes. Power levels were 25-75 watts although most of the runs were done at 50 watts power level.
Each sample was dipped immediately after plasma treatment. No studies for the effect of elapsed time (between plasma treatment and dipping) on adhesion were conducted.
Plasma treated samples for cord tensile and greige cord adhesion studies were stored in dessicators before vulcanizing and/or testing.
The plasma treated cords were passed through the adhesive dip to coat or impregnate the cords and then dried, cured or heat set in an air heated oven with 0% stretch for 90 seconds at 232° C.
The dips used were as follows:
______________________________________ Material Parts by Weight ______________________________________ Dip I Resin Master A Deionized Water 238.5 Resorcinol 11.0 NaOH 0.3 Formaldehyde (37%) 16.2 Total 266.0 Reacted at 25° C. for 6 hours Final Dip Deionized Water 60.0 Latex* 244.0 Resin Master A 266.0 NH.sub.4 OH (28%) 11.3 Total 581.3 Dip II Resin Master B Deionized Water 10.0 Phenol 95.0 NaOH 3.0 Formaldehyde (37%) 243.0 Total 351.0 Reacted at room temperature for five days or longer. Final Dip Deionized Water 314.0 Resorcinol 4.9 Resin Master B 27.9 Latex* 237.0 Total 583.8 ______________________________________ *Free radical aqueous emulsion polymerized terpolymer of about 70 parts b weight of butadiene1,3, 15 parts by weight of styrene and 15 parts by weight of 2vinyl pyridine. 41% solids, Brookfield viscosity (cps) of 30, pH of 10.7, Mooney viscosity ML4 at 212° F. of 40, surface tension (dynes/cm) of 48 and substantially freeze stable.
The dipped and dried cords were next embedded in the following rubber compound, cured for 30 minutes at 153° C. and at 20 tons ram pressure and used for the H-adhesion tests.
______________________________________ Rubber Compound Material Parts By Weight ______________________________________ Natural Rubber 46.5 SBR-1551 (free radical aqueous 38.5 emulsion, cold polymerized, copolymer of butadiene-1,3 and styrene, target bound styrene of 23.5%, nominal Mooney viscosity ML 1 + 4 (212° F.) of 52) Polybutadiene (stereospecific, 15.0 solution polymerized, 92-93% cis, nominal Mooney viscosity ML 1+ 4 at 100° C. of 45-47) Fast extruding furnace carbon black 45.0 Precipitated hydrated amorphous 15.0 silica (Hi-Sil 210, PPG Industries) Oil, highly aromatic 5.0 Zinc oxide 3.0 Stearic acid 1.5 Antioxidant (BLE, high 2.7 temperature reaction product of diphenyl amine and acetone, Uniroyal Chemical) COHEDUR RL 4.7 (a mixture of resorcinol and COHEDUR A, which is the hexa or pentamethyl ether of hexamethylol melamine, with a small amount of dibutyl phthalate plasticizer for viscosity control. Naftone, Inc.) SANTOCURE NS (N--t-butyl-2- 1.2 benzothiazolesulfenamide, Monsanto, Rubber Chemicals Div.) Sulfur (80% sulfur in oil, 3.0 CRYSTEX, Stauffer Chem.) ______________________________________
Table 1 shows data on the effect of plasma treatment on the adhesion of KEVLAR tire cord. These data show the following:
1. Both N2 and Ar plasma increased the adhesion of KEVLAR to rubber. The Ar plasma appeared to be more effective than the N2 plasma but this effect may also be at least partly due to the pressure (chamber pressure in the case of N2 was 0.70 Torr at start, increased to 1.2 torr when plasma was turned on and then decreased gradually to 0.75 torr at 15 minutes. The corresponding values for Ar plasma were 0.275 torr, 0.7 torr, and 0.30 torr, respectively).
2. With dip I as much as 50% improvement in adhesion (relative to the untreated but dipped control) was obtained, whereas with dip II the level of improvement was about 10%. This is largely because of the lower adhesion level of the dip I dipped untreated cord relative to the dip II control. This is why the dip I type dip is normally used with primer treated KEVLAR cord. Plasma treatment can, therefore, replace the primer treatment when dip I is used.
3. Plasma treated cord dipped in dip I was equivalent to the plasma treated cord dipped in dip II in terms of room temperature adhesion. The hot adhesion (121° C.) values for the dip 2 dipped cords, however, are about 10% higher than those for the corresponding dip I dipped cords.
4. As a result of plasma treatment, the mode of failure gradually shifts from cord-dip interface to predominantly rubber phase. Plasma treated dipped cords, therefore, approach the maximum adhesion level obtainable with this particular rubber compound.
TABLE 1 ______________________________________ ADHESION OF PLASMA TREATED KEVLAR CORDS ______________________________________ Treatment Conditions Time at Run Gas 50 watts Dip No. Used# (minutes) Used ______________________________________ 1 Untreated Control I 2 N.sub.2 2 I 3 N.sub.2 5 I 4 N.sub.2 10 I 5 Ar 2 I 6 Ar 5 I 7 Ar 10 I 8 Untreated Control II 9 N.sub.2 2 II 10 N.sub.2 5 II 11 N.sub.2 10 II 12 Ar 2 II 13 Ar 5 II 14 Ar 10 II ______________________________________ Run H-Adhesion (Newtons) and Mode of Failure No. RT (room temp., ca 25° C.) 121° C. ______________________________________ 1 188 Cord-dip interface 129 Cord-dip interface 2 172 Cord-dip interface -- 3 202 Some rubber -- 4 232 Some rubber -- 5 227 Some rubber -- 6 272 Mostly rubber 186 60% rubber 7 299 Mostly rubber 186 70% rubber 8 271 Mostly rubber 189 60% rubber 9 196 Cord-dip interface -- 10 263 Mostly rubber 191 80% rubber 11 280 Mostly rubber 203 80% rubber 12 258 50% rubber -- 13 285 Mostly rubber 214 90% rubber 14 294 Mostly rubber 208 90% rubber ______________________________________ #Flow rate was about 100 ml/minute.
The effect of gas flow rate on the efficacy of plasma treatment is shown in Table 2. The data show that at treatment times of 10-15 minutes, gas flow rate in the 40-100 ml/minute range does not significantly affect the adhesion level.
TABLE 2 ______________________________________ ADHESION OF PLASMA TREATED KEVLAR CORDS EFFECT OF N.sub.2 FLOW RATE Treatment Conditions Gas Time at H-Adhesions* (Newtons) and Run Flow Rate 50 watts Mode of Failure No. ml/minute (minutes) RT ______________________________________ 20 Untreated Control 232 Rubber + cord-dip interface 21 40 5 238 Rubber + cord-dip interface 22 40 10 267 Mostly rubber 23 70 5 210 Mostly cord-dip interface 24 70 15 248 Mostly rubber 25 100 5 246 Mostly rubber 26 100 15 274 Mostly rubber ______________________________________ *Dip II was used.
The effect of power level (50 watts vs. 75 watts) at treatment times of 5-15 minutes was also found not to be significant in the adhesion of KEVLAR (Table 3).
TABLE 3 ______________________________________ ADHESION OF PLASMA TREATED KEVLAR CORDS EFFECT OF POWER LEVEL Plasma Treatment Conditions* Run Power Time Relative H-Adhesion No. (watts) minutes RT 121° C. ______________________________________ 30 Untreated Control 100 100 31 50 5 108 110 32 50 8 110 33 50 12 110 34 50 20 111 111 35 75 5 111 103 36 75 8 108 37 75 12 106 38 75 20 107 107 ______________________________________ *N.sub.2 was used. Dip II was used. Gas flow rate was about 100 ml./min.
Table 4 gives data for the effect of plasma treatment on the adhesion of undipped KEVLAR to rubber. The data show that adhesion improvements obtained in this case are about 20-25% on the average. The percent improvement in this case is higher than that obtained for the dip II dipped cords (Tables 1, 2 and 3). Data in Table 4 gives a more realistic assessment of the extent of surface modification of KEVLAR as a result of plasma treatment since the matrix (rubber) strength is not the controlling factor in measured adhesion values in this case. In other KEVLAR-rubber composites, therefore, adhesion improvements of at least 20-25% may be expected as a result of plasma treatment of KEVLAR.
TABLE 4 ______________________________________ ADHESION OF PLASMA TREATED KEVLAR CORD Plasma* Treatment Conditions H-Adhesions (Newtons) and Run Gas Time Mode of Failure No. Used (minutes) RT ______________________________________ 40 Untreated Control 130 Cord-rubber interface, A 41 N.sub.2 2 147 A + some rubber 42 N.sub.2 5 162 A + some rubber 43 N.sub.2 10 160 A + some rubber 44 N.sub.2 15 157 A + some rubber 45 Ar 2 155 A + some rubber 46 Ar 5 162 A + some rubber 47 Ar 10 154 A + some rubber 48 Ar 15 175 A + some rubber ______________________________________ *50 watts power level. Gas flow rate was about 100 ml/minute.
The effect of plasma treatment on the tensile strength of undipped KEVLAR cord is shown in Table 5. These data were taken from two different sets of experiments. Relative values are shown because the values for the control cord in these two sets were not the same. The data show that the LASE [load at specified (2%) elongation] values generally decreased as the result of plasma treatment but the tensile strength and elongation to break were generally equal to or slightly better than the control. One possible explanation for these effects may be a slight reduction in the crystallinity of the cord which would tend to reduce LASE values while increasing the tensile strength and elongation to break. A reduction in the crystallinity of the cord filaments may also be at least partly responsible for adhesion improvement due to increased penetration of the adhesive into the filaments. The increase in elongation to break for multifilament KEVLAR cord was also found by Wertheimer et al6, 22. These authors, however, saw a loss of tensile strength as a result of plasma treatment. For example, these authors used microwave plasma at a frequency of 2.45 GHz and power loads of 100-700 watts and saw a tensile loss of as much as 40% after a short plasma treatment of about 1 minute in argon at 100 watts for KEVLAR. On the other hand, the present data show opposite results.
TABLE 5 ______________________________________ TENSILE PROPERTIES* OF PLASMA TREATED KEVLAR CORDS ______________________________________ Plasma Treatment Conditions# Run Gas Power Time No. Used (watts) (minutes) ______________________________________ 50 Untreated Control 51 Ar 50 2 52 Ar 50 5 53 Ar 50 10 54 N.sub.2 50 2 55 N.sub.2 50 5 56 N.sub.2 50 10 57 N.sub.2 50 20 58 N.sub.2 75 5 59 N.sub.2 75 20 ______________________________________ Relative Tensile Properties Run Load at Tensile Elongation No. 2% Elongation Strength at Break ______________________________________ 50 100 100 100 51 89 104 103 52 83 105 105 53 82 103 102 54 106 100 97 55 86-112 94-103 96-105 56 93 102 98 57 85 102 108 58 108 106 104 59 90 106 106 ______________________________________ *Measured on undipped cords. Values reported are relative to a value of 100 for the untreated control cord. #Gas flow rate was about 100 ml/minute.
Plasma treated nylon 6, 6 (hexamethylene diamine/adipic acid copolymer) cord dipped in RFL and cured in a rubber compound did not exhibit any improvement over a control (no plasma treatment). Plasma treatment reduced the tensile strength of nylon 6, 6 and polyester cords.
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Claims (28)
1. A method for adhering a poly(p-phenylene terephthalamide) reinforcing element to a rubber compound which comprises (I) treating said element with a composition comprising an aqueous alkaline dispersion of about 10 to 50% by weight of solids comprising (a) a rubbery vinyl pyridine copolymer and (b) a water soluble thermosetting phenolic-aldehyde resin in an amount of from about 3 to 25 parts by weight dry per 100 parts total by weight dry of (a), heating said treated element at a temperature of from about 200° to 600° F. for from about 300 to 5 seconds to remove essentially all of the water from said composition and to provide said element with a heat cured or heat set dry adhesive in an amount of up to about 20% total by weight (dry) based on the weight of said reinforcing element, and (II) combining said dried and heat cured adhesive containing reinforcing element with an unvulcanized vulcanizable rubber compound and vulcanizing the same, said reinforcing element prior to treatment with said composition having been treated in a cold gas plasma for from about 2 seconds to 30 minutes at from about 10 to 300 watts of power where said gas is selected from the group consisting of air, nitrogen, helium, neon and argon and mixture thereof.
2. A method according to claim 1 where said plasma is conducted from about 2 L to 20 minutes at about 25 to 75 watts of power.
3. A method according to claim 2 where said gas is nitrogen.
4. A method according to claim 2 where said gas is argon.
5. A method according to claim 1 where in (b) the resin comprises a mixture of a resorcinol-formaldehyde resin and a phenol-formaldehyde resin.
6. A method according to claim 1 where in (b) the resin comprises a resorcinol-formaldehyde resin.
7. A method according to claim 1 wherein said rubbery vinyl pyridine copolymer of (a) is a terpolymer of from about 60 to 80% by weight of butadiene-1,3, from about 7 to 32% by weight of styrene, and from about 4 to 22% by weight of 2-vinyl pyridine, wherein said phenolic-aldehyde resin of (b) is used in an amount of from about 6 to 20 parts by weight dry per 100 parts total by weight dry of (a), wherein said phenolic-aldehyde resin of (b) comprises a mixture of a phenol-formaldehyde resin and a resorcinol-formaldehyde resin, wherein said reinforcing agent contains up to about 15% total by weight of said dry adhesive and wherein the solids content of said dispersion is from about 20 to 25% by weight.
8. A method which comprises (I) treating a poly(p-phenylene terephthalamide) reinforcing element with a composition comprising an aqueous alkaline dispersion of about 10 to 50% by weight of solids comprising (a) a rubbery vinyl pyridine copolymer and (b) a water soluble thermosetting phenolic-aldehyde resin in an amount of from about 3 to 25 parts by weight dry per 100 parts total by weight dry of (a), heating said treated element at a temperature of from about 200° to 600° F. for from about 300 to 5 seconds to remove essentially all of the water from said composition and to provide said element with a heat cured or heat set dry adhesive in an amount of up to about 20% total by weight (dry) based on the weight of said reinforcing element, said reinforcing element prior to treatment with said composition having been treated in a cold gas plasma for from about 2 seconds to 30 minutes at from about 10 to 300 watts of power where said gas is selected from the group consisting of air, nitrogen, helium, neon and argon and mixture thereof.
9. A method according to claim 8 where said plasma is conducted from about 2 to 20 minutes at about 25 to 75 watts of power.
10. A method according to claim 9 where said gas is nitrogen.
11. A method according to claim 9 where said gas is argon.
12. A method according to claim 8 where in (b) the resin comprises a mixture of a resorcinol-formaldehyde resin and a phenol-formaldehyde resin.
13. A method according to claim 8 where in (b) the resin comprises a resorcinol-formaldehyde resin.
14. A method according to claim 8 wherein said rubbery vinyl pyridine copolymer of (a) is a terpolymer of from about 60 to 80% by weight of butadiene-1,3, from about 7 to 32% by weight of styrene, and from about 4 to 22% by weight of 2-vinyl pyridine, wherein said phenolic-aldehyde resin of (b) is used in an amount of from about 6 to 20 parts by weight dry per 100 parts total by weight dry of (a), wherein said phenolic-aldehyde resin of (b) comprises a mixture of a phenol-formaldehyde resin and a resorcinol-formaldehyde resin, wherein said reinforcing agent contains up to about 15% total by weight of said dry adhesive and wherein the solid contents of said dispersion is from about 20 to 25% by weight.
15. The product produced by the method of claim 1.
16. The method produced by the method of claim 2.
17. The product produced by the method of claim 3.
18. The product produced by the method of claim 4.
19. The product produced by the method of claim 5.
20. The product produced by the method of claim 6.
21. The product produced by the method of claim 7.
22. The product produced by the method of claim 8.
23. The product produced by the method of claim 9.
24. The product produced by the method of claim 10.
25. The product produced by the method of claim 11.
26. The product produced by the method of claim 12.
27. The product produced by the method of claim 13.
28. The product produced by the method of claim 14.
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US06/510,715 US4469748A (en) | 1983-07-05 | 1983-07-05 | Adhesion of aramid cords to rubber |
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Cited By (23)
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EP0168131A1 (en) * | 1984-05-25 | 1986-01-15 | Bridgestone Corporation | Method for adhering of aromatic polyamide fibers to rubber |
US4680228A (en) * | 1986-03-03 | 1987-07-14 | Gencorp Inc. | Adhesion of rubber to aramid cords |
US4783367A (en) * | 1986-05-06 | 1988-11-08 | Akzo N.V. | Fibers and yarns from a blend of aromatic polyamides |
US4820753A (en) * | 1988-03-15 | 1989-04-11 | The B. F. Goodrich Company | Acoustic window and material therefor |
FR2671113A1 (en) * | 1990-12-27 | 1992-07-03 | Michelin & Cie | PLASMA TREATMENT OF A MONOFILAMENT ARAMID AND MONOFILAMENT THUS OBTAINED. |
US5283119A (en) * | 1990-03-30 | 1994-02-01 | The Goodyear Tire & Rubber Company | Process for the surface treatment of polymers for reinforcement-to-rubber adhesion |
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US20030220427A1 (en) * | 2002-05-09 | 2003-11-27 | Gary Wentworth | Adhesion promoter for cord-reinforced rubber and metal or polymer substrate/rubber composites |
US20030220426A1 (en) * | 2002-05-09 | 2003-11-27 | Gary Wentworth | Adhesion promoter for cord-reinforced rubber and metal or polymer substrate/rubber composites |
US6696153B1 (en) * | 2000-02-03 | 2004-02-24 | Michelin Recherche Et Technique S.A. | Adhesive composition for textile/rubber adhesive bonding, and tire comprising a textile/rubber composite |
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US20040127615A1 (en) * | 2002-05-09 | 2004-07-01 | The C.P. Hall Company | Adhesion promoters for cord-reinforced thermoplastic polymeric materials and substrate/thermoplastic polymeric material composites |
US20040127616A1 (en) * | 2002-05-09 | 2004-07-01 | The C.P. Hall Company | Liquid form ester/resin adhesion promoter |
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US3853657A (en) * | 1972-02-14 | 1974-12-10 | Monsanto Co | Bonding of poly(ethylene terephthalate) induced by low-temperature plasmas |
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